Literature DB >> 11279641

Recurrent leg ulcers and arterial thrombosis in a 33-year-old homozygous variant of antithrombin.

K Shimizu1, F Toriyama, F Ogawa, I Katayama, K Okajima.   

Abstract

We report here a homozygous variant case of antithrombin (AT) associated with arterial thrombosis and recurrent leg ulcers. The deep vein thrombosis was recognized by the venogram of his pelvic veins. His leg ulcers were scattered around his left ankle and accompanied by lipodermatosclerosis, which was evident in venous insufficiency. The propositus had developed cerebral infarction 12 years prior to his leg ulcers. Coagulation study showed low heparin cofactor activity of his AT with a normal level of immunoreactive AT. Nucleotide sequence analysis of the exon 2 of his AT gene showed Arg47-Cys mutation, leading to the lack of affinity of AT for heparin. The propositus is a homozygote for this abnormality. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11279641     DOI: 10.1002/ajh.1059

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  2 in total

1.  Usefulness of antithrombin deficiency phenotypes for risk assessment of venous thromboembolism: type I deficiency as a strong risk factor for venous thromboembolism.

Authors:  Mana Mitsuguro; Toshiyuki Sakata; Akira Okamoto; Sachika Kameda; Yoshihiro Kokubo; Yoshiaki Tsutsumi; Michitaka Sano; Toshiyuki Miyata
Journal:  Int J Hematol       Date:  2010-09-23       Impact factor: 2.490

2.  Bilateral renal artery thrombosis in inherited thrombophilia: a rare cause of acute kidney injury.

Authors:  Kate S Wiles; Laura Hastings; Vasantha Muthu Muthuppalaniappan; Muhammad Hanif; Sumith Abeygunasekara
Journal:  Int J Nephrol Renovasc Dis       Date:  2014-01-18
  2 in total

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